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A Iolascon

Showing results (111-120 of 154) with videos related to

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British Journal of Haematology|March 1, 1997
Frequent de novo mutations of the ANK1 gene mimic a recessive mode of transmission in hereditary spherocytosis: three new ANK1 variants: ankyrins Bari, Napoli II and AnzioJ Randon, E Miraglia del Giudice, M Bozon, et al.
Blood Cells, Molecules & Diseases|January 8, 2011
A genomic deletion causes truncation of α-spectrin and ellipto-poikilocytosisA Iolascon, M-J King, S Robertson, et al.
European Journal of Biochemistry|March 15, 1995
Increased membrane-protein methylation in hereditary spherocytosis. A marker of cytoskeletal disarrayD Ingrosso, S D'Angelo, A F Perna, et al.
European Journal of Human Genetics : EJHG|November 28, 2000
Localisation of the gene responsible for fechtner syndrome in a region <600 Kb on 22q11-q13R Cusano, S Gangarossa, P Forabosco, et al.
Clinical and Laboratory Haematology|June 26, 2001
Flow-cytometric analysis of erythrocytes and reticulocytes in congenital dyserythropoietic anaemia type II (CDA II): value in differential diagnosis with hereditary spherocytosisP Danise, G Amendola, B Nobili, et al.
Blood|February 27, 2001
Autosomal dominant macrothrombocytopenia in Italy is most frequently a type of heterozygous Bernard-Soulier syndromeA Savoia, C L Balduini, M Savino, et al.
European Journal of Cancer (Oxford, England : 1990)|November 21, 2002
Cell division cycle control in embryonal and alveolar rhabdomyosarcomasA Moretti, A Borriello, F Monno, et al.
European Journal of Cancer (Oxford, England : 1990)|March 28, 1998
Restriction fragment length polymorphism analysis reveals different allele frequency and a linkage disequilibrium at locus D1S94 in neuroblastoma patientsP Perri, A Pession, K Mazzocco, et al.
British Journal of Haematology|December 21, 2000
Osteoporosis in beta-thalassaemia major patients: analysis of the genetic backgroundS Perrotta, M D Cappellini, F Bertoldo, et al.
British Journal of Haematology|January 1, 1993
Severe poikilocytosis associated with a de novo alpha 28 Arg-->Cys mutation in spectrinF Lorenzo, E Miraglia del Giudice, N Alloisio, et al.
Pageof 16

Showing results (111-120 of 154) with videos related to

Sort By:
Pageof 16
British Journal of Haematology|March 1, 1997
Frequent de novo mutations of the ANK1 gene mimic a recessive mode of transmission in hereditary spherocytosis: three new ANK1 variants: ankyrins Bari, Napoli II and AnzioJ Randon, E Miraglia del Giudice, M Bozon, et al.
Blood Cells, Molecules & Diseases|January 8, 2011
A genomic deletion causes truncation of α-spectrin and ellipto-poikilocytosisA Iolascon, M-J King, S Robertson, et al.
European Journal of Biochemistry|March 15, 1995
Increased membrane-protein methylation in hereditary spherocytosis. A marker of cytoskeletal disarrayD Ingrosso, S D'Angelo, A F Perna, et al.
European Journal of Human Genetics : EJHG|November 28, 2000
Localisation of the gene responsible for fechtner syndrome in a region <600 Kb on 22q11-q13R Cusano, S Gangarossa, P Forabosco, et al.
Clinical and Laboratory Haematology|June 26, 2001
Flow-cytometric analysis of erythrocytes and reticulocytes in congenital dyserythropoietic anaemia type II (CDA II): value in differential diagnosis with hereditary spherocytosisP Danise, G Amendola, B Nobili, et al.
Blood|February 27, 2001
Autosomal dominant macrothrombocytopenia in Italy is most frequently a type of heterozygous Bernard-Soulier syndromeA Savoia, C L Balduini, M Savino, et al.
European Journal of Cancer (Oxford, England : 1990)|November 21, 2002
Cell division cycle control in embryonal and alveolar rhabdomyosarcomasA Moretti, A Borriello, F Monno, et al.
European Journal of Cancer (Oxford, England : 1990)|March 28, 1998
Restriction fragment length polymorphism analysis reveals different allele frequency and a linkage disequilibrium at locus D1S94 in neuroblastoma patientsP Perri, A Pession, K Mazzocco, et al.
British Journal of Haematology|December 21, 2000
Osteoporosis in beta-thalassaemia major patients: analysis of the genetic backgroundS Perrotta, M D Cappellini, F Bertoldo, et al.
British Journal of Haematology|January 1, 1993
Severe poikilocytosis associated with a de novo alpha 28 Arg-->Cys mutation in spectrinF Lorenzo, E Miraglia del Giudice, N Alloisio, et al.
Pageof 16